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Идёт набор NCT06879730

Retrospective Evaluation of Minimally-Invasive Surgical Strategies in Ovarian Neoplasms (REMISSION Study)

Наблюдательное Early-stage Epithelial Ovarian Cancer

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Early-stage Epithelial Ovarian Cancer. Базовые параметры: Без ограничений · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Италия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

This observational study aims to evaluate the outcomes of patients with early-stage epithelial ovarian cancer who are treated with minimally invasive surgery (such as laparoscopic or robotic surgery). Specifically, the study will look at: 1. Post-Surgery Complications * What is the rate of complications within 30 days after surgery? * How often do patients require readmission to the hospital, re-operation, or conversion to open surgery? 2. Cancer Outcomes * What is the rate of cancer upstaging (when the cancer spreads to a more advanced stage during surgery for example because of an intra-operative ovarian cyst rupture)? * What are the overall survival and disease-free survival rates for patients treated with minimally invasive surgery? Researchers will compare two groups of patients: Group 1: Patients with early-stage ovarian cancer treated with minimally invasive surgery. Group 2: Patients with early-stage ovarian cancer treated with open surgery. The goal is to see if there are any differences in post-surgery complications, recovery, and cancer outcomes between the two groups. Fertility-Sparing Treatment: The study will also compare patients who are undergoing fertility-sparing treatments for early-stage ovarian cancer. Two subgroups will be looked at: * Patients receiving fertility-sparing surgery through a minimally invasive procedure. * Patients receiving fertility-sparing surgery through an open surgery. The same outcomes (complications, survival, etc.) will be assessed and compared between these two groups as well.

Первичные конечные точки

  • To assess the number of patients with 30-day post-operative complication in the two groups (minimally invasive surgery and open surgery) [Срок оценки: From surgery to post-operative day 30]
  • To assess the number of patients with 30-day post-operative hospital readmission in the two groups (minimally invasive surgery and open surgery) [Срок оценки: From surgery to post-operative day 30]
  • To assess the number of patients with 30-day post-operative reoperation in the two groups (minimally invasive surgery and open surgery) [Срок оценки: From surgery to post-operative day 30]
  • To assess the rate of upstaging in the two groups (minimally invasive surgery and open surgery) [Срок оценки: At the time of surgery]
  • To assess the rate of conversion in the minimally invasive surgery group [Срок оценки: At the time of surgery]
Вторичные конечные точки (1)
  • To analyze predictor of recurrence and oncological outcomes in terms of disease-free survival (DFS) and overall survival (OS) in the minimally invasive surgery and in the open surgery groups [Срок оценки: From the date of surgery to the date of the last follow-up or the date of recurrence/death, whichever occurs first, assessed up to 300 weeks]

Критерии участия

Критерии включения

  • Patients with apparent early-stage epithelial ovarian cancer at preoperative evaluation
  • Patients who underwent surgery between January 2014 and December 2023
  • Patients who underwent open or minimally invasive surgical staging (Laparoscopic or Robotic-assisted approach) or restaging procedure
  • Patients with final pathology report of Epithelial Ovarian Cancer

Критерии исключения

  • Patients who have not performed a complete surgical staging
  • Patients who underwent neoadjuvant chemotherapy
  • Patients with invasive synchronous tumor
  • Patients with no informed consent
  • Patients with ASA class score of 4 or 5

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Случай-контроль

Центры проведения

Италия · 1 центр
  • Ospedale Filippo del Ponte — Varese

Идентификаторы

NCT: NCT06879730 · 55/2024

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗